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Management of Severely Atrophic Maxilla in Ectrodactyly Ectodermal Dysplasia-cleft Syndrome.

作者信息

Rachmiel Adi, Turgeman Shahar, Emodi Omri, Aizenbud Dror, Shilo Dekel

机构信息

Department of Oral and Maxillofacial Surgery, Rambam Health Care Campus, Haifa, Israel; Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel; and Department of Orthodontics and Cleft Palate, Rambam Health Care Campus, Haifa, Israel.

出版信息

Plast Reconstr Surg Glob Open. 2018 Feb 27;6(2):e1678. doi: 10.1097/GOX.0000000000001678. eCollection 2018 Feb.

DOI:10.1097/GOX.0000000000001678
PMID:29616174
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5865928/
Abstract

BACKGROUND

Ectrodactyly ectodermal dysplasia-cleft syndrome is a rare genetic syndrome with an incidence of 1/90,000 live births, characterized by cleft lip and palate, severely hypoplastic maxilla, and hypodontia. Patients diagnosed with ectrodactyly ectodermal dysplasia-cleft syndrome suffer from a severely hypoplastic maxilla that is highly difficult to treat using traditional orthognathic methods. In this study, we propose using distraction osteogenesis to achieve a major advancement while maintaining good stability and minimal relapse. To our knowledge, this is the first description of patients with this syndrome treated using distraction osteogenesis.

METHODS

Five patients diagnosed with ectrodactyly ectodermal dysplasia-cleft syndrome were included in the study. All patients had been operated on according to the well-established protocol of cleft lip and palate reconstruction before maxillary distraction osteogenesis. Hard and soft-tissue changes were evaluated by cone beam computed tomography and lateral cephalograms before distraction osteogenesis (T1), at the postdistraction point (T2) and after 1 year of follow-up (T3).

RESULTS

Examination revealed marked maxillary advancement in all our patients with a significant mean difference in hard tissue parameters (condylion to A point = 18 mm; nasion-sella line to A point = 15.2 degrees) and a notable improvement in facial convexity (20.9 degrees). One year follow-up measurements demonstrated mild relapse rates of 6% in the horizontal plane.

CONCLUSIONS

We conclude that despite the challenging anatomic and physiological features of ectrodactyly ectodermal dysplasia-cleft patients, by enhancing current surgical techniques, there is promising potential for improved patient outcomes, achieving normognathic facial appearance with implant supported rehabilitation.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/45498b448ee2/gox-6-e1678-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/68ba9641d3dd/gox-6-e1678-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/3e362b302d6f/gox-6-e1678-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/5fb2acf281bf/gox-6-e1678-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/2091e3002752/gox-6-e1678-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/a06cd9553e5d/gox-6-e1678-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/20da8b7c5ee7/gox-6-e1678-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/9def74f7c335/gox-6-e1678-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/45498b448ee2/gox-6-e1678-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/68ba9641d3dd/gox-6-e1678-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/3e362b302d6f/gox-6-e1678-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/5fb2acf281bf/gox-6-e1678-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/2091e3002752/gox-6-e1678-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/a06cd9553e5d/gox-6-e1678-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/20da8b7c5ee7/gox-6-e1678-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/9def74f7c335/gox-6-e1678-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e426/5865928/45498b448ee2/gox-6-e1678-g009.jpg

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本文引用的文献

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Ann Maxillofac Surg. 2016 Jul-Dec;6(2):214-218. doi: 10.4103/2231-0746.200319.
2
Stability after Cleft Maxillary Distraction Osteogenesis or Conventional Orthognathic Surgery.腭裂上颌骨牵张成骨术或传统正颌外科手术后的稳定性。
J Oral Maxillofac Res. 2015 Jun 30;6(2):e2. doi: 10.5037/jomr.2015.6202. eCollection 2015 Apr-Jun.
3
Ectrodactyly, Ectodermal Dysplasia, Cleft Lip, and Palate (EEC Syndrome) with Tetralogy of Fallot: A Very Rare Combination.
并指(趾)畸形、外胚层发育不良、唇腭裂(EEC 综合征)合并法洛四联症:非常罕见的组合。
Front Pediatr. 2015 Jun 16;3:51. doi: 10.3389/fped.2015.00051. eCollection 2015.
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Le fort I maxillary advancement using distraction osteogenesis.上颌骨强力推进术采用牵张成骨术。
Semin Plast Surg. 2014 Nov;28(4):193-8. doi: 10.1055/s-0034-1390172.
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Treatment of maxillary cleft palate: Distraction osteogenesis vs. orthognathic surgery.上颌腭裂的治疗:牵张成骨术与正颌外科手术
Ann Maxillofac Surg. 2012 Jul;2(2):127-30. doi: 10.4103/2231-0746.101336.
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Oral and dental restoration of wide alveolar cleft using distraction osteogenesis and temporary anchorage devices.采用牵张成骨和临时固定装置对宽牙槽嵴裂进行口腔和牙齿修复。
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Treatment of severe hypodontia-oligodontia--an interdisciplinary concept.严重牙列稀疏-少牙畸形的治疗——一个跨学科理念。
Int J Oral Maxillofac Surg. 2007 Jun;36(6):473-80. doi: 10.1016/j.ijom.2007.01.021. Epub 2007 Apr 12.
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Cleft maxillary distraction versus orthognathic surgery: clinical morbidities and surgical relapse.上颌骨腭裂牵张成骨术与正颌外科手术:临床发病率及手术复发情况
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